Ectopic Overexpression of CsECR From Navel Orange Increases Cuticular Wax Accumulation in Tomato and Enhances Its Tolerance to Drought Stress

Drought stress often occurred in citrus to limit its growth, distribution, and fruit quality. Cuticular waxes play an important role in regulating plant tolerance to drought stress. Plant enoyl-CoA reductase (ECR) is involved in the biosynthesis of cuticular waxes and catalyzes the last step of very...

Full description

Saved in:
Bibliographic Details
Published inFrontiers in plant science Vol. 13; p. 924552
Main Authors Liu, Dechun, Guo, Wenfang, Guo, Xinyue, Yang, Li, Hu, Wei, Kuang, Liuqing, Huang, Yingjie, Xie, Jingheng, Liu, Yong
Format Journal Article
LanguageEnglish
Published Frontiers Media S.A 05.07.2022
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Drought stress often occurred in citrus to limit its growth, distribution, and fruit quality. Cuticular waxes play an important role in regulating plant tolerance to drought stress. Plant enoyl-CoA reductase (ECR) is involved in the biosynthesis of cuticular waxes and catalyzes the last step of very long-chain fatty acids (VLCFAs) elongation. In this study, a putative ECR gene, named CsECR , was cloned from “Newhall” navel orange. CsECR protein has high identities with other plant ECR proteins and contained a conserved NADP/NAD-binding motif and three conserved functional sites. The highest expression of CsECR was observed in leaves, followed by stems, flavedos, ovaries, juice sacs, stigmas, stamens, albedos, and petals. Besides, the expression of CsECR was significantly induced by PEG6000 and ABA treatments. Ectopic overexpression of CsECR increased the contents of total waxes and aliphatic wax fractions ( n -fatty acids, unsaturated fatty acids, n -alkanes, alkenes, iso-, and anteiso-alkanes) in the leaves and fruits of the transgenic tomato. Furthermore, ectopic overexpression of CsECR reduced the cuticle permeability in the leaves and fruits of the transgenic tomato and increased its tolerance to drought stress. Taken together, our results revealed that CsECR plays an important role in plant response to drought stresses by regulating cuticular wax biosynthesis.
AbstractList Drought stress often occurred in citrus to limit its growth, distribution, and fruit quality. Cuticular waxes play an important role in regulating plant tolerance to drought stress. Plant enoyl-CoA reductase (ECR) is involved in the biosynthesis of cuticular waxes and catalyzes the last step of very long-chain fatty acids (VLCFAs) elongation. In this study, a putative ECR gene, named CsECR , was cloned from “Newhall” navel orange. CsECR protein has high identities with other plant ECR proteins and contained a conserved NADP/NAD-binding motif and three conserved functional sites. The highest expression of CsECR was observed in leaves, followed by stems, flavedos, ovaries, juice sacs, stigmas, stamens, albedos, and petals. Besides, the expression of CsECR was significantly induced by PEG6000 and ABA treatments. Ectopic overexpression of CsECR increased the contents of total waxes and aliphatic wax fractions ( n -fatty acids, unsaturated fatty acids, n -alkanes, alkenes, iso-, and anteiso-alkanes) in the leaves and fruits of the transgenic tomato. Furthermore, ectopic overexpression of CsECR reduced the cuticle permeability in the leaves and fruits of the transgenic tomato and increased its tolerance to drought stress. Taken together, our results revealed that CsECR plays an important role in plant response to drought stresses by regulating cuticular wax biosynthesis.
Drought stress often occurred in citrus to limit its growth, distribution, and fruit quality. Cuticular waxes play an important role in regulating plant tolerance to drought stress. Plant enoyl-CoA reductase (ECR) is involved in the biosynthesis of cuticular waxes and catalyzes the last step of very long-chain fatty acids (VLCFAs) elongation. In this study, a putative ECR gene, named CsECR, was cloned from "Newhall" navel orange. CsECR protein has high identities with other plant ECR proteins and contained a conserved NADP/NAD-binding motif and three conserved functional sites. The highest expression of CsECR was observed in leaves, followed by stems, flavedos, ovaries, juice sacs, stigmas, stamens, albedos, and petals. Besides, the expression of CsECR was significantly induced by PEG6000 and ABA treatments. Ectopic overexpression of CsECR increased the contents of total waxes and aliphatic wax fractions (n-fatty acids, unsaturated fatty acids, n-alkanes, alkenes, iso-, and anteiso-alkanes) in the leaves and fruits of the transgenic tomato. Furthermore, ectopic overexpression of CsECR reduced the cuticle permeability in the leaves and fruits of the transgenic tomato and increased its tolerance to drought stress. Taken together, our results revealed that CsECR plays an important role in plant response to drought stresses by regulating cuticular wax biosynthesis.Drought stress often occurred in citrus to limit its growth, distribution, and fruit quality. Cuticular waxes play an important role in regulating plant tolerance to drought stress. Plant enoyl-CoA reductase (ECR) is involved in the biosynthesis of cuticular waxes and catalyzes the last step of very long-chain fatty acids (VLCFAs) elongation. In this study, a putative ECR gene, named CsECR, was cloned from "Newhall" navel orange. CsECR protein has high identities with other plant ECR proteins and contained a conserved NADP/NAD-binding motif and three conserved functional sites. The highest expression of CsECR was observed in leaves, followed by stems, flavedos, ovaries, juice sacs, stigmas, stamens, albedos, and petals. Besides, the expression of CsECR was significantly induced by PEG6000 and ABA treatments. Ectopic overexpression of CsECR increased the contents of total waxes and aliphatic wax fractions (n-fatty acids, unsaturated fatty acids, n-alkanes, alkenes, iso-, and anteiso-alkanes) in the leaves and fruits of the transgenic tomato. Furthermore, ectopic overexpression of CsECR reduced the cuticle permeability in the leaves and fruits of the transgenic tomato and increased its tolerance to drought stress. Taken together, our results revealed that CsECR plays an important role in plant response to drought stresses by regulating cuticular wax biosynthesis.
Drought stress often occurred in citrus to limit its growth, distribution, and fruit quality. Cuticular waxes play an important role in regulating plant tolerance to drought stress. Plant enoyl-CoA reductase (ECR) is involved in the biosynthesis of cuticular waxes and catalyzes the last step of very long-chain fatty acids (VLCFAs) elongation. In this study, a putative ECR gene, named CsECR, was cloned from “Newhall” navel orange. CsECR protein has high identities with other plant ECR proteins and contained a conserved NADP/NAD-binding motif and three conserved functional sites. The highest expression of CsECR was observed in leaves, followed by stems, flavedos, ovaries, juice sacs, stigmas, stamens, albedos, and petals. Besides, the expression of CsECR was significantly induced by PEG6000 and ABA treatments. Ectopic overexpression of CsECR increased the contents of total waxes and aliphatic wax fractions (n-fatty acids, unsaturated fatty acids, n-alkanes, alkenes, iso-, and anteiso-alkanes) in the leaves and fruits of the transgenic tomato. Furthermore, ectopic overexpression of CsECR reduced the cuticle permeability in the leaves and fruits of the transgenic tomato and increased its tolerance to drought stress. Taken together, our results revealed that CsECR plays an important role in plant response to drought stresses by regulating cuticular wax biosynthesis.
Author Xie, Jingheng
Kuang, Liuqing
Liu, Dechun
Yang, Li
Hu, Wei
Guo, Xinyue
Liu, Yong
Huang, Yingjie
Guo, Wenfang
AuthorAffiliation Department of Pomology, College of Agronomy, Jiangxi Agricultural University , Nanchang , China
AuthorAffiliation_xml – name: Department of Pomology, College of Agronomy, Jiangxi Agricultural University , Nanchang , China
Author_xml – sequence: 1
  givenname: Dechun
  surname: Liu
  fullname: Liu, Dechun
– sequence: 2
  givenname: Wenfang
  surname: Guo
  fullname: Guo, Wenfang
– sequence: 3
  givenname: Xinyue
  surname: Guo
  fullname: Guo, Xinyue
– sequence: 4
  givenname: Li
  surname: Yang
  fullname: Yang, Li
– sequence: 5
  givenname: Wei
  surname: Hu
  fullname: Hu, Wei
– sequence: 6
  givenname: Liuqing
  surname: Kuang
  fullname: Kuang, Liuqing
– sequence: 7
  givenname: Yingjie
  surname: Huang
  fullname: Huang, Yingjie
– sequence: 8
  givenname: Jingheng
  surname: Xie
  fullname: Xie, Jingheng
– sequence: 9
  givenname: Yong
  surname: Liu
  fullname: Liu, Yong
BookMark eNp1kk1vEzEQhleoiJbSO0cfuSR4_bX2BakKKUSqiASR4GY59myy1a4dbG_U_gj-M96mQhQJX-yZ8fuMP97X1ZkPHqrqbY3nlEr1vj30aU4wIXNFGOfkRXVRC8FmTJAfZ3-tz6urlO5wGRxjpZpX1TnlUnAixUX1a2lzOHQWrY8Q4f4QIaUueBRatEjLxVd0E8OAvpgj9Ggdjd8BWnkbwSRIaDHmzo69iei7uUfX1o5DifKk7zzahMHkgIx3aOn3xtuiWOVU8j3EKUSl-jGGcbfP6FueOr-pXramT3D1NF9Wm5vlZvF5drv-tFpc384soyrPqHOqlZywVgolwfFGKofZVnLeUADXMicpM8oIKA9T16amFmNoMGEg1ZZeVqsT1gVzpw-xG0x80MF0-jER4k6bWK7Wg7Z0W8tatVsrHWtqp4QCMLxRigpMlCysDyfWYdwO4Cz4HE3_DPq84ru93oWjVkQxRUgBvHsCxPBzhJT10CULfW88hDFpIhRtGl6LpmzFp602hpQitH_a1FhPntCTJ_TkCX3yRJGIfyS2y49fVA7T9f8X_gaAFL7u
CitedBy_id crossref_primary_10_3390_ijms241210235
crossref_primary_10_3390_biotech11040048
crossref_primary_10_1111_jipb_13739
crossref_primary_10_1093_jxb_erad321
crossref_primary_10_3390_ijms25116106
crossref_primary_10_3390_ijms232315053
crossref_primary_10_1007_s10725_022_00905_x
crossref_primary_10_3390_genes13091591
crossref_primary_10_1093_jxb_erae319
crossref_primary_10_3390_ijms241813876
crossref_primary_10_3389_fpls_2024_1333286
Cites_doi 10.1016/j.plaphy.2021.09.032
10.1105/tpc.11.5.825
10.1105/tpc.107.054858
10.1093/genetics/149.2.607
10.1016/j.foodchem.2013.12.021
10.1093/jxb/erp057
10.1093/jxb/erab420
10.1007/s11103-011-9861-2
10.3389/fpls.2017.00621
10.1093/jxb/47.12.1813
10.1104/pp.112.210450
10.1016/j.foodchem.2020.127684
10.1002/jsfa.2740260913
10.1186/1471-2229-10-230
10.1093/hr/uhac004
10.1021/jf00055a015
10.1046/j.1365-313X.1999.00352.x
10.1007/s11295-016-1017-8
10.1016/j.plaphy.2021.06.045
10.1007/s11103-007-9150-2
10.3389/fpls.2018.01869
10.1007/s11103-008-9339-z
10.1007/s11103-015-0343-9
10.1016/j.plaphy.2020.12.032
10.1016/j.postharvbio.2009.07.005
10.3389/fpls.2019.00431
10.1007/s00299-005-0084-3
10.1007/s12033-017-0014-y
10.2307/40537768
10.1104/pp.109.137497
10.1016/j.jplph.2010.11.014
10.1007/s00299-015-1772-2
10.1093/treephys/tpaa079
10.1093/pcp/pcu142
10.1093/jxb/erh061
10.1104/pp.20.00603
10.1104/pp.109.141911
10.1111/j.1365-313X.2009.03973.x
10.1016/j.febslet.2005.07.013
10.1016/j.hpj.2018.11.003
10.1128/MCB.21.1.109-125.2001
10.1074/jbc.M701774200
10.2307/25680057
10.1046/j.1365-313x.1997.12010121.x
10.1105/tpc.111.083485
10.3390/molecules25020412
10.3390/ijms23105660
10.1104/pp.107.099481
10.1016/j.scienta.2010.06.015
10.1111/j.1469-8137.2006.01826.x
10.1038/s41438-018-0051-0
10.1105/tpc.114.123307
10.1080/10942912.2018.1528272
10.1016/j.plantsci.2013.05.008
10.1007/s00425-019-03115-4
10.1016/j.plantsci.2015.12.010
10.1007/s11738-009-0404-2
10.3390/ijms151119499
10.1105/tpc.104.030155
10.2307/20205718
10.1111/pce.13614
10.1016/S1875-2780(11)60012-6
10.1111/j.1365-313x.2005.02418.x
10.1093/jxb/erh149
10.3389/fpls.2020.564656
10.1007/s00299-012-1333-x
10.1073/pnas.0805089105
ContentType Journal Article
Copyright Copyright © 2022 Liu, Guo, Guo, Yang, Hu, Kuang, Huang, Xie and Liu.
Copyright © 2022 Liu, Guo, Guo, Yang, Hu, Kuang, Huang, Xie and Liu. 2022 Liu, Guo, Guo, Yang, Hu, Kuang, Huang, Xie and Liu
Copyright_xml – notice: Copyright © 2022 Liu, Guo, Guo, Yang, Hu, Kuang, Huang, Xie and Liu.
– notice: Copyright © 2022 Liu, Guo, Guo, Yang, Hu, Kuang, Huang, Xie and Liu. 2022 Liu, Guo, Guo, Yang, Hu, Kuang, Huang, Xie and Liu
DBID AAYXX
CITATION
7X8
5PM
DOA
DOI 10.3389/fpls.2022.924552
DatabaseName CrossRef
MEDLINE - Academic
PubMed Central (Full Participant titles)
DOAJ Open Access Full Text
DatabaseTitle CrossRef
MEDLINE - Academic
DatabaseTitleList CrossRef
MEDLINE - Academic


Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
DeliveryMethod fulltext_linktorsrc
Discipline Botany
EISSN 1664-462X
ExternalDocumentID oai_doaj_org_article_c3b1819fbc8d471d969eea5799360298
PMC9294922
10_3389_fpls_2022_924552
GrantInformation_xml – fundername: ;
  grantid: 31701896; 31860544
– fundername: ;
– fundername: ;
  grantid: 2019YFD1000100
GroupedDBID 5VS
9T4
AAFWJ
AAKDD
AAYXX
ACGFO
ACGFS
ACXDI
ADBBV
ADRAZ
AENEX
AFPKN
ALMA_UNASSIGNED_HOLDINGS
AOIJS
BCNDV
CITATION
EBD
ECGQY
GROUPED_DOAJ
GX1
HYE
KQ8
M48
M~E
OK1
PGMZT
RNS
RPM
7X8
5PM
ID FETCH-LOGICAL-c439t-3dd9f8524f8698ed5789d04b85573eedf4d834a9a6e45511a13c00e7024e89b3
IEDL.DBID DOA
ISSN 1664-462X
IngestDate Wed Aug 27 01:21:03 EDT 2025
Thu Aug 21 17:50:14 EDT 2025
Fri Jul 11 00:37:06 EDT 2025
Tue Jul 01 00:37:17 EDT 2025
Thu Apr 24 23:04:15 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Language English
License This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c439t-3dd9f8524f8698ed5789d04b85573eedf4d834a9a6e45511a13c00e7024e89b3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
This article was submitted to Plant Metabolism and Chemodiversity, a section of the journal Frontiers in Plant Science
Reviewed by: Adoración Zafra, Spanish National Research Council (CSIC), Spain; Nazim Hussain, Independent Researcher, Sharjah, United Arab Emirates
Edited by: Agnieszka Zienkiewicz, Nicolaus Copernicus University in Toruń, Poland
OpenAccessLink https://doaj.org/article/c3b1819fbc8d471d969eea5799360298
PMID 35865286
PQID 2693775167
PQPubID 23479
ParticipantIDs doaj_primary_oai_doaj_org_article_c3b1819fbc8d471d969eea5799360298
pubmedcentral_primary_oai_pubmedcentral_nih_gov_9294922
proquest_miscellaneous_2693775167
crossref_primary_10_3389_fpls_2022_924552
crossref_citationtrail_10_3389_fpls_2022_924552
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2022-07-05
PublicationDateYYYYMMDD 2022-07-05
PublicationDate_xml – month: 07
  year: 2022
  text: 2022-07-05
  day: 05
PublicationDecade 2020
PublicationTitle Frontiers in plant science
PublicationYear 2022
Publisher Frontiers Media S.A
Publisher_xml – name: Frontiers Media S.A
References Wang (B58) 2012; 78
Shepherd (B50) 2006; 171
Xue (B61) 2017
Raffaele (B45) 2008; 20
Joubès (B17) 2008; 67
Vogg (B54) 2004; 55
Kim (B19) 2013; 162
Kosma (B22) 2009; 151
Dan (B7) 2006; 25
Kohlwein (B20) 2001; 21
Ni (B40) 2011; 37
Ding (B10) 2020; 25
Todd (B52) 1999; 17
Paul (B43) 2007; 282
Millar (B37) 1999; 11
Zhang (B64) 2022; 73
Zhou (B67) 2021
Wu (B60) 2022
Go (B12) 2014; 26
He (B15) 2018
Zhang (B62) 2020; 40
Millar (B38) 1997; 12
Roudier (B47) 2010; 22
Baker (B3) 1975; 26
Song (B51) 2009; 60
Huang (B16) 2010
Liu (B30) 2010; 32
Liu (B33) 2015; 88
Kerstiens (B18) 1996; 47
Lee (B25); 56
Liu (B32) 2016; 12
Liu (B31) 2021; 167
Bach (B2) 2008; 105
Park (B42) 2005; 579
Wen (B59) 2021; 166
Leide (B26) 2007; 144
Guo (B13) 2020
Lee (B24); 34
Cajuste (B6) 2010; 55
Ding (B9) 2018; 21
Kong (B21) 2020; 183
Seo (B49) 2009; 151
Beaudoin (B4) 2009; 150
Wang (B55) 2021; 159
Haslam (B14) 2013; 210
Liang (B29) 2022; 23
Dietrich (B8) 2005; 42
Nordby (B41) 1995; 43
Li (B28) 2019; 42
Zhang (B65) 2019; 249
Gable (B11) 2004; 55
Brewer (B5) 2006; 141
Al-Abdallat (B1) 2014; 15
Lolle (B36) 1998; 149
Lee (B23) 2009; 60
Leide (B27) 2011; 168
Lokesh (B35) 2019
Trivedi (B53) 2019
Rodríguez-Gamir (B46) 2010; 126
Zhang (B63) 2007; 64
Wang (B57) 2015; 243
Liu (B34) 2012; 31
Mustafa (B39) 2017; 59
Seo (B48) 2011; 23
Wang (B56) 2014; 153
Qi (B44) 2019; 5
Zheng (B66) 2005; 17
References_xml – volume: 167
  start-page: 1049
  year: 2021
  ident: B31
  article-title: Comparative analysis of the cuticular waxes and related gene expression between ‘Newhall' and ‘Ganqi 3' navel orange during long-term cold storage
  publication-title: Plant Physiol. Biochem
  doi: 10.1016/j.plaphy.2021.09.032
– volume: 11
  start-page: 825
  year: 1999
  ident: B37
  article-title: CUT1, an Arabidopsis gene required for cuticular wax biosynthesis and pollen fertility, encodes a very-long-chain fatty acid condensing enzyme
  publication-title: Plant Cell
  doi: 10.1105/tpc.11.5.825
– volume: 20
  start-page: 752
  year: 2008
  ident: B45
  article-title: A MYB transcription factor regulates very-long-chain fatty acid biosynthesis for activation of the hypersensitive cell death response in Arabidopsis
  publication-title: Plant Cell
  doi: 10.1105/tpc.107.054858
– volume: 149
  start-page: 607
  year: 1998
  ident: B36
  article-title: Genetic analysis of organ fusion in Arabidopsis thaliana
  publication-title: Genetics
  doi: 10.1093/genetics/149.2.607
– volume: 153
  start-page: 177
  year: 2014
  ident: B56
  article-title: Comparative analysis of surface wax in mature fruits between Satsuma mandarin (Citrus unshiu) and ‘Newhall' navel orange (Citrus sinensis) from the perspective of crystal morphology, chemical composition and key gene expression
  publication-title: Food Chem
  doi: 10.1016/j.foodchem.2013.12.021
– volume: 60
  start-page: 1839
  year: 2009
  ident: B51
  article-title: Characterization of two cotton cDNAs encoding trans-2-enoyl-CoA reductase reveals a putative novel NADPH-binding motif
  publication-title: J. Exp. Bot
  doi: 10.1093/jxb/erp057
– volume: 73
  start-page: 953
  year: 2022
  ident: B64
  article-title: CsMYB96 confers water loss resistance in citrus fruit by simultaneous regulation of water transport and wax biosynthesis
  publication-title: J. Exp. Bot
  doi: 10.1093/jxb/erab420
– volume: 78
  start-page: 275
  year: 2012
  ident: B58
  article-title: An ethylene response factor OsWR1 responsive to drought stress transcriptionally activates wax synthesis related genes and increases wax production in rice
  publication-title: Plant Mol. Biol
  doi: 10.1007/s11103-011-9861-2
– year: 2017
  ident: B61
  article-title: Molecular and evolutionary mechanisms of cuticular wax for plant drought tolerance
  publication-title: Front. Plant Sci
  doi: 10.3389/fpls.2017.00621
– volume: 47
  start-page: 1813
  year: 1996
  ident: B18
  article-title: Cuticular water permeability and its physiological significance
  publication-title: J. Exp. Bot
  doi: 10.1093/jxb/47.12.1813
– volume: 162
  start-page: 567
  year: 2013
  ident: B19
  article-title: Arabidopsis 3-ketoacyl-coenzyme A synthase 9 is involved in the synthesis of tetracosanoic acids as precursors of cuticular waxes, suberins, sphingolipids, and phospholipids
  publication-title: Plant Physiol
  doi: 10.1104/pp.112.210450
– year: 2021
  ident: B67
  article-title: Variations of membrane fatty acids and epicuticular wax metabolism in response to oleocellosis in lemon fruit
  publication-title: Food Chem
  doi: 10.1016/j.foodchem.2020.127684
– volume: 26
  start-page: 1093
  year: 1975
  ident: B3
  article-title: The cuticles of citrus species. Composition of leaf and fruit waxes
  publication-title: J. Sci. Food Agr
  doi: 10.1002/jsfa.2740260913
– year: 2010
  ident: B16
  article-title: Overexpression of PtrABF gene, a bZIP transcription factor isolated from Poncirus trifoliata, enhances dehydration and drought tolerance in tobacco via scavenging ROS and modulating expression of stress-responsive genes
  publication-title: BMC Plant Biol
  doi: 10.1186/1471-2229-10-230
– year: 2022
  ident: B60
  article-title: Tomato SlCER1–1 catalyzes the synthesis of wax alkanes, increasing drought tolerance and fruit storability
  publication-title: Hortic. Res
  doi: 10.1093/hr/uhac004
– volume: 43
  start-page: 1828
  year: 1995
  ident: B41
  article-title: Variations in chilling injury and epicuticular wax composition of white grapefruit with canopy position and fruit development during the season
  publication-title: J. Agr. Food Chem
  doi: 10.1021/jf00055a015
– volume: 17
  start-page: 119
  year: 1999
  ident: B52
  article-title: KCS1 encodes a fatty acid elongase3-ketoacyl-CoA synthase affecting wax biosynthesis in Arabidopsis thaliana
  publication-title: Plant J
  doi: 10.1046/j.1365-313X.1999.00352.x
– volume: 12
  start-page: 55
  year: 2016
  ident: B32
  article-title: Transcriptome sequencing identified wax-related genes controlling the glossy phenotype formation of “Ganqi 3,” a bud mutant derived from wild-type “Newhall” navel orange
  publication-title: Tree Genet. Genomes
  doi: 10.1007/s11295-016-1017-8
– volume: 166
  start-page: 777
  year: 2021
  ident: B59
  article-title: Ectopic expression of CsMYB30 from Citrus sinensis enhances salt and drought tolerance by regulating wax synthesis in Arabidopsis thaliana
  publication-title: Plant Physiol. Bioch
  doi: 10.1016/j.plaphy.2021.06.045
– volume: 64
  start-page: 265
  year: 2007
  ident: B63
  article-title: Heterologous expression of two Medicago truncatula putative ERF transcription factor genes, WXP1 and WXP2, in Arabidopsis led to increased leaf wax accumulation and improved drought tolerance, but differential response in freezing tolerance
  publication-title: Plant Mol. Biol
  doi: 10.1007/s11103-007-9150-2
– year: 2019
  ident: B35
  article-title: Overexpression of ß-Ketoacyl Co-A synthase1 gene improves tolerance of drought susceptible groundnut (Arachis hypogaea L.) cultivar K-6 by increased leaf epicuticular wax accumulation
  publication-title: Front. Plant Sci
  doi: 10.3389/fpls.2018.01869
– volume: 67
  start-page: 547
  year: 2008
  ident: B17
  article-title: The VLCFA elongase gene family in Arabidopsis thaliana: phylogenetic analysis, 3D modelling and expression profiling
  publication-title: Plant Mol. Biol.
  doi: 10.1007/s11103-008-9339-z
– volume: 88
  start-page: 573
  year: 2015
  ident: B33
  article-title: Analysis of cuticular wax constituents and genes that contribute to the formation of ‘glossy Newhall', a spontaneous bud mutant from the wild-type ‘Newhall' navel orange
  publication-title: Plant Mol. Biol
  doi: 10.1007/s11103-015-0343-9
– volume: 159
  start-page: 312
  year: 2021
  ident: B55
  article-title: Poa pratensis ECERIFERUM1 (PpCER1) is involved in wax alkane biosynthesis and plant drought tolerance
  publication-title: Plant Physiol. Bioch
  doi: 10.1016/j.plaphy.2020.12.032
– volume: 55
  start-page: 29
  year: 2010
  ident: B6
  article-title: Epicuticular wax content and morphology as related to ethylene and storage performance of ‘Navelate' orange fruit
  publication-title: Postharvest Biol. Technol
  doi: 10.1016/j.postharvbio.2009.07.005
– year: 2019
  ident: B53
  article-title: Developmental and environmental regulation of cuticular wax biosynthesis in fleshy fruits
  publication-title: Front. Plant Sci
  doi: 10.3389/fpls.2019.00431
– volume: 25
  start-page: 432
  year: 2006
  ident: B7
  article-title: MicroTom-a high-throughput model transformation system for functional genomics
  publication-title: Plant Cell Rep
  doi: 10.1007/s00299-005-0084-3
– volume: 59
  start-page: 241
  year: 2017
  ident: B39
  article-title: Tobacco rattle virus-based silencing of Enoyl-CoA reductase gene and its role in resistance against cotton wilt disease
  publication-title: Mol. Biotechnol
  doi: 10.1007/s12033-017-0014-y
– volume: 151
  start-page: 275
  year: 2009
  ident: B49
  article-title: The MYB96 transcription factor mediates abscisic acid signaling during drought stress response in Arabidopsis
  publication-title: Plant Physiol
  doi: 10.2307/40537768
– volume: 150
  start-page: 1174
  year: 2009
  ident: B4
  article-title: Functional characterization of the Arabidopsis thaliana β-ketoacyl-CoA reductase candidates of the fatty acid elongase
  publication-title: Plant Physiol
  doi: 10.1104/pp.109.137497
– volume: 168
  start-page: 871
  year: 2011
  ident: B27
  article-title: The positional sterile (ps) mutation affects cuticular transpiration and wax biosynthesis of tomato fruits
  publication-title: J. Plant Physiol.
  doi: 10.1016/j.jplph.2010.11.014
– volume: 34
  start-page: 557
  ident: B24
  article-title: Advances in the understanding of cuticular waxes in Arabidopsis thaliana and crop species
  publication-title: Plant Cell Rep
  doi: 10.1007/s00299-015-1772-2
– volume: 40
  start-page: 1450
  year: 2020
  ident: B62
  article-title: An apple long-chain acyl-CoA synthetase 2 gene enhances plant resistance to abiotic stress by regulating the accumulation of cuticular wax
  publication-title: Tree Physiol
  doi: 10.1093/treephys/tpaa079
– volume: 56
  start-page: 48
  ident: B25
  article-title: Cuticular wax biosynthesis is up-regulated by the MYB94 transcription factor in Arabidopsis
  publication-title: Plant Cell Physiol
  doi: 10.1093/pcp/pcu142
– volume: 55
  start-page: 543
  year: 2004
  ident: B11
  article-title: Functional characterization of the Arabidopsis thaliana orthologue of Tsc13p, the enoyl reductase of the yeast microsomal fatty acid elongating system
  publication-title: J. Exp. Bot
  doi: 10.1093/jxb/erh061
– volume: 183
  start-page: 1250
  year: 2020
  ident: B21
  article-title: Epigenetic activation of enoyl-CoA reductase by an acetyltransferase complex triggers wheat wax biosynthesis
  publication-title: Plant Physiol
  doi: 10.1104/pp.20.00603
– volume: 151
  start-page: 1918
  year: 2009
  ident: B22
  article-title: The impact of water deficiency on leaf cuticle lipids of Arabidopsis
  publication-title: Plant Physiol
  doi: 10.1104/pp.109.141911
– volume: 60
  start-page: 462
  year: 2009
  ident: B23
  article-title: Two Arabidopsis 3-ketoacyl CoA synthase genes, KCS20 and KCS2/DAISY, are functionally redundant in cuticular wax and root suberin biosynthesis, but diferentially controlled by osmotic stress
  publication-title: Plant J
  doi: 10.1111/j.1365-313X.2009.03973.x
– volume: 579
  start-page: 4459
  year: 2005
  ident: B42
  article-title: Silencing of NbECR encoding a putative enoyl-CoA reductase results in disorganized membrane structures and epidermal cell ablation in Nicotiana benthamiana
  publication-title: FEBS Lett
  doi: 10.1016/j.febslet.2005.07.013
– volume: 5
  start-page: 1
  year: 2019
  ident: B44
  article-title: The characterization, authentication, and gene expression pattern of the MdCER family in Malus domestica
  publication-title: Hortic. Plant J
  doi: 10.1016/j.hpj.2018.11.003
– volume: 21
  start-page: 109
  year: 2001
  ident: B20
  article-title: Tsc13p is required for fatty acid elongation and localizes to a novel structure at the nuclear-vacuolar interface in Saccharomyces cerevisiae
  publication-title: Mol. Cell Biol
  doi: 10.1128/MCB.21.1.109-125.2001
– volume: 282
  start-page: 19237
  year: 2007
  ident: B43
  article-title: A six-membrane-spanning topology for yeast and Arabidopsis Tsc13p, the enoyl reductases of the microsomal fatty acid elongating system
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.M701774200
– volume: 22
  start-page: 364
  year: 2010
  ident: B47
  article-title: Very-long-chain fatty acids are involved in polar auxin transport and developmental patterning in Arabidopsis
  publication-title: Plant Cell
  doi: 10.2307/25680057
– volume: 12
  start-page: 121
  year: 1997
  ident: B38
  article-title: Very-long-chain fatty acid biosynthesis is controlled through the expression and specificity of the condensing enzyme
  publication-title: Plant J
  doi: 10.1046/j.1365-313x.1997.12010121.x
– volume: 23
  start-page: 1138
  year: 2011
  ident: B48
  article-title: The MYB96 transcription factor regulates cuticular wax biosynthesis under drought conditions in Arabidopsis
  publication-title: Plant Cell
  doi: 10.1105/tpc.111.083485
– volume: 25
  start-page: 412
  year: 2020
  ident: B10
  article-title: Changes in cuticle components and morphology of ‘Satsuma' Mandarin (Citrus unshiu) during ambient storage and their potential role on Penicillium digitatum infection
  publication-title: Molecules
  doi: 10.3390/molecules25020412
– volume: 23
  start-page: 5660
  year: 2022
  ident: B29
  article-title: Transcriptome and physiological analyses of a navel orange mutant with improved drought tolerance and water use efficiency caused by increases of cuticular wax accumulation and ROS scavenging capacity
  publication-title: Int. J. Mol. Sci
  doi: 10.3390/ijms23105660
– volume: 144
  start-page: 1667
  year: 2007
  ident: B26
  article-title: The developmental pattern of tomato fruit wax accumulation and its impact on cuticular transpiration barrier properties: effects of a deficiency in a β-ketoacyl-coenzyme A synthase (LeCER6)
  publication-title: Plant Physiol.
  doi: 10.1104/pp.107.099481
– volume: 126
  start-page: 95
  year: 2010
  ident: B46
  article-title: Citrus rootstock responses to water stress
  publication-title: Sci. Hortic
  doi: 10.1016/j.scienta.2010.06.015
– volume: 171
  start-page: 469
  year: 2006
  ident: B50
  article-title: The effects of stress on plant cuticular waxes
  publication-title: New Phytol
  doi: 10.1111/j.1469-8137.2006.01826.x
– year: 2018
  ident: B15
  article-title: Integrated transcriptomic and metabolomic analyses of a wax deficient citrus mutant exhibiting jasmonic acid-mediated defense against fungal pathogens
  publication-title: Hortic. Res
  doi: 10.1038/s41438-018-0051-0
– volume: 26
  start-page: 1666
  year: 2014
  ident: B12
  article-title: Arabidopsis cuticular wax biosynthesis is negatively regulated by the DEWAX gene encoding an AP2/ERF-type transcription factor
  publication-title: Plant Cell
  doi: 10.1105/tpc.114.123307
– volume: 21
  start-page: 2411
  year: 2018
  ident: B9
  article-title: Changes in cuticle compositions and crystal structure of ‘Bingtang' sweet orange fruits (Citrus sinensis) during storage
  publication-title: Int. J. Food Prop
  doi: 10.1080/10942912.2018.1528272
– volume: 210
  start-page: 93
  year: 2013
  ident: B14
  article-title: Extending the story of very-long-chain fatty acid elongation
  publication-title: Plant Sci
  doi: 10.1016/j.plantsci.2013.05.008
– volume: 249
  start-page: 1627
  year: 2019
  ident: B65
  article-title: Apple AP2/EREBP transcription factor MdSHINE2 confers drought resistance by regulating wax biosynthesis
  publication-title: Planta
  doi: 10.1007/s00425-019-03115-4
– volume: 243
  start-page: 131
  year: 2015
  ident: B57
  article-title: Regulation of cuticle formation during fruit development and ripening in ‘Newhall' navel orange (Citrus sinensis Osbeck) revealed by transcriptomic and metabolomic profiling
  publication-title: Plant Science
  doi: 10.1016/j.plantsci.2015.12.010
– volume: 32
  start-page: 271
  year: 2010
  ident: B30
  article-title: Molecular cloning, characterization and expression analysis of PtrHOS1, a novel gene of cold responses from trifoliate orange [Poncirus trifoliata (L.) Raf.]
  publication-title: Acta Physiol. Plant
  doi: 10.1007/s11738-009-0404-2
– volume: 15
  start-page: 19499
  year: 2014
  ident: B1
  article-title: Over-expression of SlSHN1 gene improves drought tolerance by increasing cuticular wax accumulation in tomato
  publication-title: Int. J. Mol. Sci
  doi: 10.3390/ijms151119499
– volume: 17
  start-page: 1467
  year: 2005
  ident: B66
  article-title: Disruptions of the Arabidopsis enoyl-CoA reductase gene reveal an essential role for very-long-chain fatty acid synthesis in cell expansion during plant morphogenesis
  publication-title: Plant Cell
  doi: 10.1105/tpc.104.030155
– volume: 141
  start-page: 15
  year: 2006
  ident: B5
  article-title: Development of a controlled vocabulary and software application to analyze fruit shape variation in tomato and other plant species
  publication-title: Plant Physiol
  doi: 10.2307/20205718
– volume: 42
  start-page: 3077
  year: 2019
  ident: B28
  article-title: TaCER1-1A is involved in cuticular wax alkane biosynthesis in hexaploid wheat and responds to plant abiotic stresses
  publication-title: Plant Cell Environ
  doi: 10.1111/pce.13614
– volume: 37
  start-page: 424
  year: 2011
  ident: B40
  article-title: Cloning and functional analysis of enoyl-CoA reductase gene BnECR from oilseed rape (Brassica napus L.)
  publication-title: Acta Agron. Sin
  doi: 10.1016/S1875-2780(11)60012-6
– volume: 42
  start-page: 844
  year: 2005
  ident: B8
  article-title: Characterization of two GL8 paralogs reveals that the 3-ketoacyl reductase component of fatty acid elongase is essential for maize (Zea mays L.) development
  publication-title: Plant J.
  doi: 10.1111/j.1365-313x.2005.02418.x
– volume: 55
  start-page: 1401
  year: 2004
  ident: B54
  article-title: Tomato fruit cuticular waxes and their effects on transpiration barrier properties: functional characterization of a mutant deficient in a very-long-chain fatty acid β-ketoacyl-CoA synthase
  publication-title: J. Exp. Bot.
  doi: 10.1093/jxb/erh149
– year: 2020
  ident: B13
  article-title: Ectopic expression of CsKCS6 from navel orange promotes the production of very-long-chain fatty acids (VLCFAs) and increases the abiotic stress tolerance of Arabidopsis thaliana
  publication-title: Front. Plant Sci
  doi: 10.3389/fpls.2020.564656
– volume: 31
  start-page: 2239
  year: 2012
  ident: B34
  article-title: A comparison of the ultrastructure and composition of fruit' cuticular wax from the wild-type ‘Newhall' navel orange (Citrus sinensis [L.] Osbeck cv. Newhall) and its glossy mutant
  publication-title: Plant Cell Rep
  doi: 10.1007/s00299-012-1333-x
– volume: 105
  start-page: 14727
  year: 2008
  ident: B2
  article-title: The very-long-chain hydroxy fatty acyl-CoA dehydratase PASTICCINO2 is essential and limiting for plant development
  publication-title: Proc. Natl. Acad. Sci. U. S. A.
  doi: 10.1073/pnas.0805089105
SSID ssj0000500997
Score 2.400816
Snippet Drought stress often occurred in citrus to limit its growth, distribution, and fruit quality. Cuticular waxes play an important role in regulating plant...
SourceID doaj
pubmedcentral
proquest
crossref
SourceType Open Website
Open Access Repository
Aggregation Database
Enrichment Source
Index Database
StartPage 924552
SubjectTerms CsECR
cuticular wax
drought
navel orange
Plant Science
transgenic tomato
SummonAdditionalLinks – databaseName: Scholars Portal Journals: Open Access
  dbid: M48
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1La9wwEBYl6aGX0ifdvphALz048UPPQynJdpe0kATaDc3NyJKcLDj21vaWzY_If-7IdtIYQk-96oFszYzmGzT6hpAPsVY6kpoG3CY8oEawQCthgzCXUmdC5HFXzufomB-e0m9n7Ozv8-hhA5t7QztfT-q0LnY3v64-o8F_8hEn-tu9fFV44u043sVggjE8kLfRLwlvpkcD2O-Zvj0cEv1d5b0TR76po_Af4c5x1uQdNzR_Qh4P-BH2e4E_JQ9c-Yw8PKgQ4109J9cz01arpYET1FC3GZJcS6hymDaz6XeY19UlHOvfroCT2r8rADwgfF66a2C67og4dA0_9Qb2jVlfDrW9YFnCokJsW4EuLczKC68rDXxtG2wvnC_O4QB7v3RFf1r40b1AeUEW89liehgMBRcCg7ikDRJrVS5ZTHPJlXQWrVnZkGaSMZGgM82plQlF6XKH2xVFOkpMGDqBft5JlSUvyVZZle4VgcRyaVlicUJE8QjDsCym2iLcUizMuZyQvZudTs1ARu5rYhQpBiVeNqmXTeplk_aymZCPtzNWPRHHP8YeeOHdjvMU2l1DVZ-ng0WmJskQ3ag8M9Kih7aKK-c0EwjYuOeln5CdG9GnaHL-HkWXrlrjShwxnWARFxMiRjoxWnHcUy4vOvJuhKNUxfHr__GJb8gj_9dd9jB7S7baeu3eIUZqs_ed6v8BlXIR7Q
  priority: 102
  providerName: Scholars Portal
Title Ectopic Overexpression of CsECR From Navel Orange Increases Cuticular Wax Accumulation in Tomato and Enhances Its Tolerance to Drought Stress
URI https://www.proquest.com/docview/2693775167
https://pubmed.ncbi.nlm.nih.gov/PMC9294922
https://doaj.org/article/c3b1819fbc8d471d969eea5799360298
Volume 13
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Lb9QwELZQxYEL4imWAhokLhzCJvH72G532yK1lWARe4sc21FX2iar3SwqP4L_zNhJq82FXrj44Niy4xl7vpHH3xDyKTfaZMqwRDgqEmYlT4yWLkkrpUwpZZXHdD4Xl-LsB_u64Iu9VF8hJqyjB-4WbmxpiUZIV6VVDg9Sp4X23nCJdlUE-vBw-qLN23OmOlbvAH1kdy-JXpgeV-tVYOfO8y_ocXCeD-xQpOsfYMxhhOSeyZk9I097rAhH3Ryfk0e-fkEeHzeI536_JH-mtm3WSwtXqI3-tg9oraGpYLKdTr7BbNPcwKX55VdwtQlvCAAPgxCD7rcw2UXSDbOBn-YWjqzd3fR5vGBZw7xBHNuAqR1M6-ugF1s4b7dYv_IhEYcH_HoSE_y08D2-NnlF5rPpfHKW9MkVEosYpE2oc7pSPGeVElp5hztXu5SVinNJ0XBWzCnKUJLC43JlmcmoTVMv0aZ7pUv6mhzUTe3fEKBOKMepww4Zw-MKXbCcGYfQSvO0EmpExncrXdieeDzkv1gV6IAE2RRBNkWQTdHJZkQ-3_dYd6Qb_2h7HIR33y7QZccKVKKiV6LiISUakY93oi9we4U7E1P7ZocjCcRvkmdCjogc6MRgxOGXenkdiboRejKd52__xxQPyZPw1zFSmL8jB-1m598jHmrLD1H1sTxdZFheMPUXudILhQ
linkProvider Directory of Open Access Journals
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Ectopic+Overexpression+of+CsECR+From+Navel+Orange+Increases+Cuticular+Wax+Accumulation+in+Tomato+and+Enhances+Its+Tolerance+to+Drought+Stress&rft.jtitle=Frontiers+in+plant+science&rft.au=Dechun+Liu&rft.au=Wenfang+Guo&rft.au=Xinyue+Guo&rft.au=Li+Yang&rft.date=2022-07-05&rft.pub=Frontiers+Media+S.A&rft.eissn=1664-462X&rft.volume=13&rft_id=info:doi/10.3389%2Ffpls.2022.924552&rft.externalDBID=DOA&rft.externalDocID=oai_doaj_org_article_c3b1819fbc8d471d969eea5799360298
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1664-462X&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1664-462X&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1664-462X&client=summon